메뉴 건너뛰기




Volumn 106, Issue 2, 2005, Pages 531-533

Accelerated telomere shortening in glycosylphosphatidylinositol (GPI)-negative compared with GPI-positive granulocytes from patients with paroxysmal nocturnal hemoglobinuria (PNH) detected by proaerolysin flow-FISH

Author keywords

[No Author keywords available]

Indexed keywords

AEROLYSIN; DYE; GLYCOSYLPHOSPHATIDYLINOSITOL; PROAEROLYSIN; UNCLASSIFIED DRUG;

EID: 22144437035     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2004-10-3996     Document Type: Article
Times cited : (35)

References (25)
  • 1
    • 0014832992 scopus 로고
    • Paroxysmal nocturnal hemoglobinuria: Evidence for monoclonal origin of abnormal red cells
    • Oni SB, Osunkoya BO, Luzzatto L. Paroxysmal nocturnal hemoglobinuria: evidence for monoclonal origin of abnormal red cells. Blood. 1970;36:145-152.
    • (1970) Blood , vol.36 , pp. 145-152
    • Oni, S.B.1    Osunkoya, B.O.2    Luzzatto, L.3
  • 2
    • 0028057807 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene
    • Bessler M, Mason PJ, Hillmen P, et al. Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene. EMBO J. 1994;13:110-117.
    • (1994) EMBO. , vol.13 , pp. 110-117
    • Bessler, M.1    Mason, P.J.2    Hillmen, P.3
  • 3
    • 0027412627 scopus 로고
    • The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis
    • Miyata T, Takeda J, Iida Y, et al. The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis. Science. 1993;259:1318-1320.
    • (1993) Science , vol.259 , pp. 1318-1320
    • Miyata, T.1    Takeda, J.2    Iida, Y.3
  • 5
    • 0015515155 scopus 로고
    • Origin of concatemeric T7 DNA
    • Watson JD. Origin of concatemeric T7 DNA. Nat New Biol. 1972;239:197-201.
    • (1972) Nat New Biol , vol.239 , pp. 197-201
    • Watson, J.D.1
  • 8
    • 0030829892 scopus 로고    scopus 로고
    • Telomerase in human development and cancer
    • Shay JW. Telomerase in human development and cancer. J Cell Physiol. 1997;173:266-270.
    • (1997) J Cell Physiol , vol.173 , pp. 266-270
    • Shay, J.W.1
  • 9
    • 0038494897 scopus 로고    scopus 로고
    • Severe telomere shortening in patients with paroxysmal nocturnal hemoglobinuria affects both GPI- and GPU+ hematopoiesis
    • Karadimitris A, Araten DJ, Luzzatto L, Notaro R. Severe telomere shortening in patients with paroxysmal nocturnal hemoglobinuria affects both GPI- and GPU+ hematopoiesis. Blood. 2003;102:514-516.
    • (2003) Blood , vol.102 , pp. 514-516
    • Karadimitris, A.1    Araten, D.J.2    Luzzatto, L.3    Notaro, R.4
  • 10
    • 0032525092 scopus 로고    scopus 로고
    • Progressive telomere shortening in aplastic anemia
    • Ball SE, Gibson FM, Rizzo S, et al. Progressive telomere shortening in aplastic anemia. Blood. 1998;91:3582-3592.
    • (1998) Blood , vol.91 , pp. 3582-3592
    • Ball, S.E.1    Gibson, F.M.2    Rizzo, S.3
  • 11
    • 0035865618 scopus 로고    scopus 로고
    • Telomere length in leukocyte subpopulations of patients with aplastic anemia
    • Brummendorf TH, Maciejewski JP, Mak J, Young NS, Lansdorp PM. Telomere length in leukocyte subpopulations of patients with aplastic anemia. Blood. 2001;97:895-900.
    • (2001) Blood , vol.97 , pp. 895-900
    • Brummendorf, T.H.1    Maciejewski, J.P.2    Mak, J.3    Young, N.S.4    Lansdorp, P.M.5
  • 12
    • 0141484361 scopus 로고    scopus 로고
    • Cytogenetic abnormalities in paroxysmal nocturnal haemoglobinuria usually occur in haematopoietic cells that are glycosylphosphatidylinositol-anchored protein (GPI-AP) positive
    • Sloand EM, Fuhrer M, Keyvanfar K, et al. Cytogenetic abnormalities in paroxysmal nocturnal haemoglobinuria usually occur in haematopoietic cells that are glycosylphosphatidylinositol-anchored protein (GPI-AP) positive. Br J Haematol. 2003;123:173-176.
    • (2003) Br J Haematol , vol.123 , pp. 173-176
    • Sloand, E.M.1    Fuhrer, M.2    Keyvanfar, K.3
  • 13
    • 0345643319 scopus 로고    scopus 로고
    • Telomere fluorescence measurements in granulocytes and T lymphocyte subsets point to a high turnover of hematopoietic stem cells and memory T cells in early childhood
    • Rufer N, Brummendorf TH, Kolvraa S, et al. Telomere fluorescence measurements in granulocytes and T lymphocyte subsets point to a high turnover of hematopoietic stem cells and memory T cells in early childhood. J Exp Med. 1999;190:157-167.
    • (1999) J Exp Med , vol.190 , pp. 157-167
    • Rufer, N.1    Brummendorf, T.H.2    Kolvraa, S.3
  • 14
    • 84925548155 scopus 로고    scopus 로고
    • Telomere length measurement by fluorescence in situ hybridization and flow cytometry: Tips and pitfalls
    • Baerlocher GM, Mak J, Tien T, Lansdorp PM. Telomere length measurement by fluorescence in situ hybridization and flow cytometry: tips and pitfalls. Cytometry. 2002;47:89-99.
    • (2002) Cytometry , vol.47 , pp. 89-99
    • Baerlocher, G.M.1    Mak, J.2    Tien, T.3    Lansdorp, P.M.4
  • 15
    • 0033105696 scopus 로고    scopus 로고
    • Resistance of paroxysmal nocturnal hemoglobinuria cells to the glycosylphosphatidylinositol-binding toxin aerolysin
    • Brodsky RA, Mukhina GL, Nelson KL, et al. Resistance of paroxysmal nocturnal hemoglobinuria cells to the glycosylphosphatidylinositol-binding toxin aerolysin. Blood. 1999;93:1749-1756.
    • (1999) Blood , vol.93 , pp. 1749-1756
    • Brodsky, R.A.1    Mukhina, G.L.2    Nelson, K.L.3
  • 16
    • 0035166456 scopus 로고    scopus 로고
    • Simultaneous flow cytometric analysis of cell surface markers and telomere length: Analysis of human tonsilar B cells
    • Batliwalla FM, Damle RN, Metz C, Chiorazzi N, Gregersen PK. Simultaneous flow cytometric analysis of cell surface markers and telomere length: analysis of human tonsilar B cells. J Immunol Methods. 2001;247:103-109.
    • (2001) J Immunol Methods , vol.247 , pp. 103-109
    • Batliwalla, F.M.1    Damle, R.N.2    Metz, C.3    Chiorazzi, N.4    Gregersen, P.K.5
  • 17
    • 4444380656 scopus 로고    scopus 로고
    • Telomere length analysis by fluorescence in situ hybridization and flow cytometry (flow-FISH)
    • Hartmann U, Beier F, Brummendorf TH. Telomere length analysis by fluorescence in situ hybridization and flow cytometry (flow-FISH). J Lab Med. 2004;28:307-316.
    • (2004) J Lab Med , vol.28 , pp. 307-316
    • Hartmann, U.1    Beier, F.2    Brummendorf, T.H.3
  • 18
    • 0034966374 scopus 로고    scopus 로고
    • Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita
    • Vulliamy TJ, Knight SW, Mason PJ, Dokal I. Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita. Blood Cells Mol Dis. 2001;27:353-357.
    • (2001) Blood Cells Mol Dis , vol.27 , pp. 353-357
    • Vulliamy, T.J.1    Knight, S.W.2    Mason, P.J.3    Dokal, I.4
  • 19
    • 0033518188 scopus 로고    scopus 로고
    • A telomerase component is defective in the human disease dyskeratosis congenita
    • Mitchell JR, Wood E, Collins K. A telomerase component is defective in the human disease dyskeratosis congenita. Nature. 1999;402:551-555.
    • (1999) Nature , vol.402 , pp. 551-555
    • Mitchell, J.R.1    Wood, E.2    Collins, K.3
  • 20
    • 0035960043 scopus 로고    scopus 로고
    • The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
    • Vulliamy T, Marrone A, Goldman F, et al. The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature. 2001;413:432-435.
    • (2001) Nature , vol.413 , pp. 432-435
    • Vulliamy, T.1    Marrone, A.2    Goldman, F.3
  • 21
    • 0344851536 scopus 로고    scopus 로고
    • Late presentation of dyskeratosis congenita as apparently acquired aplastic anaemia due to mutations in telomerase RNA
    • Fogarty PF, Yamaguchi H, Wiestner A, et al. Late presentation of dyskeratosis congenita as apparently acquired aplastic anaemia due to mutations in telomerase RNA. Lancet. 2003;362:1628-1630.
    • (2003) Lancet , vol.362 , pp. 1628-1630
    • Fogarty, P.F.1    Yamaguchi, H.2    Wiestner, A.3
  • 22
    • 0041592752 scopus 로고    scopus 로고
    • Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome
    • Yamaguchi H, Baerlocher GM, Lansdorp PM, et al. Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome. Blood. 2003;102:916-918.
    • (2003) Blood , vol.102 , pp. 916-918
    • Yamaguchi, H.1    Baerlocher, G.M.2    Lansdorp, P.M.3
  • 23
    • 13144281829 scopus 로고    scopus 로고
    • A mutation in a functional Sp1 binding site of the telomerase RNA gene (hTERC) promoter in a patient with paroxysmal nocturnal haemoglobinuria
    • Keith WN, Vulliamy T, Zhao J, et al. A mutation in a functional Sp1 binding site of the telomerase RNA gene (hTERC) promoter in a patient with paroxysmal nocturnal haemoglobinuria. BMC Blood Disord. 2004;4:3.
    • (2004) BMC Blood Disord , vol.4 , pp. 3
    • Keith, W.N.1    Vulliamy, T.2    Zhao, J.3
  • 24
    • 0034502010 scopus 로고    scopus 로고
    • Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin
    • Brodsky RA, Mukhina GL, Li S, et al. Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin. Am J Clin Pathol. 2000;114:459-466.
    • (2000) Am J Clin Pathol , vol.114 , pp. 459-466
    • Brodsky, R.A.1    Mukhina, G.L.2    Li, S.3
  • 25
    • 0035726553 scopus 로고    scopus 로고
    • Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria
    • Araten DJ, Swirsky D, Karadimitris A, et al. Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria. Br J Haematol. 2001;115:360-368.
    • (2001) Br J Haematol , vol.115 , pp. 360-368
    • Araten, D.J.1    Swirsky, D.2    Karadimitris, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.